Canonical Allele Identifier: CA340729248

Gene: IL23R

Linked Data

• MyVariant Identifiers: chr1:g.67724609T>C (hg19) ; chr1:g.67258926T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67258926T>C , CM000663.2:g.67258926T>C	GRCh38
NC_000001.10:g.67724609T>C , CM000663.1:g.67724609T>C	GRCh37
NC_000001.9:g.67497197T>C	NCBI36
NG_011498.1:g.97441T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697149.1:c.1527T>C	ENSP00000513138.1:n.1527T>C
ENST00000697150.1:c.1585T>C	ENSP00000513139.1:n.1585T>C
ENST00000697151.1:c.1518T>C	ENSP00000513140.1:n.1518T>C
ENST00000697164.1:c.1598T>C	ENSP00000513153.1:p.Ile533Thr
ENST00000697165.1:c.1385T>C	ENSP00000513154.1:p.Ile462Thr
ENST00000347310.10:c.1688T>C MANE Select	ENSP00000321345.5:p.Ile563Thr
ENST00000637002.1:c.1079T>C	ENSP00000490340.1:p.Ile360Thr
ENST00000347310.9:c.1688T>C	ENSP00000321345.5:p.Ile563Thr
ENST00000395227.2:c.482T>C	ENSP00000378652.2:p.Ile161Thr
ENST00000425614.3:c.923T>C	ENSP00000387640.2:p.Ile308Thr
ENST00000473881.2:c.*514T>C	ENSP00000486667.1:n.*514T>C
NM_144701.2:c.1688T>C	NP_653302.2:p.Ile563Thr
XM_005270516.2:c.926T>C	XP_005270573.1:p.Ile309Thr
XM_011540789.1:c.1778T>C	XP_011539091.1:p.Ile593Thr
XM_011540790.1:c.1688T>C	XP_011539092.1:p.Ile563Thr
XM_011540791.1:c.1688T>C	XP_011539093.1:p.Ile563Thr
XM_011540790.3:c.1688T>C	XP_011539092.1:p.Ile563Thr
XM_011540791.3:c.1688T>C	XP_011539093.1:p.Ile563Thr
XR_001736993.1:n.1768T>C
NM_144701.3:c.1688T>C MANE Select	NP_653302.2:p.Ile563Thr